United States · FDA National Drug Code directory
Prednisolone Sodium Phosphate Oral Solution
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 44523-182_450e8d3f-b6f6-5251-e063-6394a90aa439
- Product NDC
- 44523-182
- Form
- SOLUTION
- Composition / generic term
- Prednisolone Sodium Phosphate
- Labeler
- BioComp Pharma, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20191028
- Source listing expiry
- 20261231
Source-listed ingredients
- PREDNISOLONE SODIUM PHOSPHATE — 25 mg/5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 237 mL in 1 BOTTLE (44523-182-08) · 44523-182-08
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →